Primary Site >> Stomach Cancer
Gene >> PLCE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94246526:94246526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376113551 |
| CDS Mutation | c.3001G>A |
| AA Mutation | p.Gly1001Arg(p.G1001R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94279879:94279879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4763A>G |
| AA Mutation | p.Glu1588Gly(p.E1588G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031687:94031687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.641G>T |
| AA Mutation | p.Gly214Val(p.G214V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94324418:94324418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6571G>A |
| AA Mutation | p.Glu2191Lys(p.E2191K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94255022:94255022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3527T>G |
| AA Mutation | p.Leu1176Arg(p.L1176R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94254214:94254214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763011760 |
| CDS Mutation | c.3304G>A |
| AA Mutation | p.Asp1102Asn(p.D1102N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94306614:94306614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5810G>A |
| AA Mutation | p.Arg1937His(p.R1937H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94262691:94262691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4012G>A |
| AA Mutation | p.Gly1338Arg(p.G1338R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94270580:94270580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771124727 |
| CDS Mutation | c.4484G>A |
| AA Mutation | p.Arg1495Gln(p.R1495Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94171227:94171227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1540A>C |
| AA Mutation | p.Ser514Arg(p.S514R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94316725:94316725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6311T>C |
| AA Mutation | p.Met2104Thr(p.M2104T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031198:94031198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152C>T |
| AA Mutation | p.Ser51Phe(p.S51F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94324423:94324423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6576G>T |
| AA Mutation | p.Glu2192Asp(p.E2192D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031117:94031117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775247624 |
| CDS Mutation | c.71C>T |
| AA Mutation | p.Ser24Leu(p.S24L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031585:94031585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539C>A |
| AA Mutation | p.Pro180His(p.P180H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031928:94031928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.882G>T |
| AA Mutation | p.Lys294Asn(p.K294N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260766 |
| Start | 94321939:94321939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6381G>T |
| AA Mutation | p.Glu2127Asp(p.E2127D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94246225:94246225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2700C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94265886:94265886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145456568 |
| CDS Mutation | c.4209C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94132185:94132185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031817:94031817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.771C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94227338:94227338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771344723 |
| CDS Mutation | c.1842G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94304552:94304552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5529A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94273645:94273645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4590A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94032099:94032099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1053G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94252372:94252372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3153C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94171346:94171346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1659C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94246138:94246138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94031139:94031139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.93A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94293617:94293617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5145A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260766 |
| Start | 94246076:94246076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2551C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260766 |
| Start | 94227386:94227386(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1890delT |
| AA Mutation | p.His630GlnfsTer28(p.H630Qfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260766 |
| Start | 94265814:94265814(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4140delT |
| AA Mutation | p.Phe1380LeufsTer43(p.F1380Lfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260766 |
| Start | 94316591:94316591(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6182delT |
| AA Mutation | p.Leu2061Ter(p.L2061*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260766 |
| Start | 94254950:94254950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3455T>A |
| AA Mutation | p.Leu1152Ter(p.L1152*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260766 |
| Start | 94306685:94306685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774196868 |
| CDS Mutation | c.5881C>T |
| AA Mutation | p.Arg1961Ter(p.R1961*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |